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Unblinded, randomized multicenter trial comparing lamotrigine and valproate combination with controlled-release carbamazepine monotherapy as initial drug regimen in untreated epilepsy

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dc.contributor.authorLee, Byung In-
dc.contributor.authorNo, Soon Kee-
dc.contributor.authorYi, Sang-Doe-
dc.contributor.authorLee, Hyang Woon-
dc.contributor.authorKim, Ok Joon-
dc.contributor.authorKim, Sang Ho-
dc.contributor.authorKim, Myeong Kyu-
dc.contributor.authorKim, Sung Eun-
dc.contributor.authorKim, Yo Sik-
dc.contributor.authorKim, Jae Moon-
dc.contributor.authorLee, Se-Jin-
dc.contributor.authorShin, Dong Jin-
dc.contributor.authorPark, Sung Pa-
dc.contributor.authorKim, Yeong In-
dc.contributor.authorHeo, Kyoung-
dc.contributor.authorCho, Yong Won-
dc.contributor.authorCho, Yang-Je-
dc.contributor.authorKim, Youn Nam-
dc.date.available2020-02-27T11:42:45Z-
dc.date.created2020-02-06-
dc.date.issued2018-02-
dc.identifier.issn1059-1311-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4115-
dc.description.abstractPurpose: To compare controlled-release carbamazepine monotherapy (CBZ-CR) with lamotrigine and valproate combination therapy (LTG + VPA) in equivalent total drug load, as initial drug regimen in untreated patients with partial and/or generalized tonic-clonic seizures (GTCS). Methods: This unblinded, randomized, 60-week superiority trial recruited patients having two or more unprovoked seizures with at least one seizure during previous three months. After randomization into CBZ-CR or LTG + VPA, patients entered into eight-week titration phase (TP), followed by 52-week maintenance phase (MP). Median doses of CBZ-CR and LTG + VPA were 600 mg/day and 75 mg/day, + 500 mg/day, respectively. Primary outcome measure was completion rate (CR), a proportion of patients who have completed the 60-week study as planned. Secondary efficacy measures included seizure-free rate (SFR) for 52-week of MP and time to first seizure (TTFS) during MP. Results: Among 207 randomized patients, 202 underwent outcome analysis (104 in CBZ-CR, 98 in LTG + VPA). CR was 62.5% in CBZ-CR and 65.3% in LTG + VPA (p = 0.678). SFR during MP was higher in LTG + VPA (64.1%) than CBZ-CR (47.8%) (P = 0.034). TTFS was shorter with CBZ-CR (p = 0.041). Incidence of adverse effects (AEs) were 57.7% in CBZ-CR and 60.2% in LTG + VPA and premature drug withdrawal rates due to AEs were 12.5% and 7.1%, respectively, which were not significantly different. Conclusion: CR was comparable between LTG + VPA and CBZ-CR, however, both SFR for 52-week MP and TTFS during MP were in favor of LTG + VPA than CBZ-CR. The study suggested that LTG + VPA can be an option as initial drug regimen for untreated patients with partial seizures and/or GTCS except for women of reproductive age. (C) 2017 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherW B SAUNDERS CO LTD-
dc.relation.isPartOfSEIZURE-EUROPEAN JOURNAL OF EPILEPSY-
dc.subjectANTIEPILEPTIC DRUGS-
dc.subjectADJUNCTIVE THERAPY-
dc.subjectPOLYTHERAPY-
dc.subjectEFFICACY-
dc.subjectSUBSTITUTION-
dc.subjectPREGNANCY-
dc.subjectSEIZURES-
dc.subjectPLACE-
dc.subjectWOMEN-
dc.subjectRASH-
dc.titleUnblinded, randomized multicenter trial comparing lamotrigine and valproate combination with controlled-release carbamazepine monotherapy as initial drug regimen in untreated epilepsy-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000430644800004-
dc.identifier.doi10.1016/j.seizure.2017.12.008-
dc.identifier.bibliographicCitationSEIZURE-EUROPEAN JOURNAL OF EPILEPSY, v.55, pp.17 - 24-
dc.identifier.scopusid2-s2.0-85043358392-
dc.citation.endPage24-
dc.citation.startPage17-
dc.citation.titleSEIZURE-EUROPEAN JOURNAL OF EPILEPSY-
dc.citation.volume55-
dc.contributor.affiliatedAuthorShin, Dong Jin-
dc.type.docTypeArticle-
dc.subject.keywordAuthorMonotherapy-
dc.subject.keywordAuthorCombination therapy-
dc.subject.keywordAuthorCBZ-CR-
dc.subject.keywordAuthorLTG plus VPA-
dc.subject.keywordAuthorInitial drug regimen-
dc.subject.keywordPlusANTIEPILEPTIC DRUGS-
dc.subject.keywordPlusADJUNCTIVE THERAPY-
dc.subject.keywordPlusPOLYTHERAPY-
dc.subject.keywordPlusEFFICACY-
dc.subject.keywordPlusSUBSTITUTION-
dc.subject.keywordPlusPREGNANCY-
dc.subject.keywordPlusSEIZURES-
dc.subject.keywordPlusPLACE-
dc.subject.keywordPlusWOMEN-
dc.subject.keywordPlusRASH-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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